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methionine and Congenital Disorders of Glycosylation

methionine has been researched along with Congenital Disorders of Glycosylation in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Barić, I; Bauerová, L; Belužić, R; Elleder, M; Hansíkova, H; Honzík, T; Ješina, P; Kožich, V; Krijt, J; Magner, M; Ondrušková, N; Sokolová, J; Veselá, K; Vugrek, O; Zeman, J1
Aronica, E; Poll-The, BT; Rozemuller-Kwakkel, JM; Troost, D; van der Heide, M; van Kempen, AA; van Slooten, HJ1
Hanefeld, F; Holzbach, U; Knauer, R; Körner, C; Lehle, L; von Figura, K1

Other Studies

3 other study(ies) available for methionine and Congenital Disorders of Glycosylation

ArticleYear
Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency.
    Molecular genetics and metabolism, 2012, Volume: 107, Issue:3

    Topics: Adenosylhomocysteinase; Congenital Disorders of Glycosylation; Diagnosis, Differential; Erythrocytes; Female; Fibroblasts; Heterozygote; Homocysteine; Humans; Infant, Newborn; Methionine; Mutation; Phosphotransferases (Phosphomutases)

2012
Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology.
    Acta neuropathologica, 2005, Volume: 109, Issue:4

    Topics: Arginine; Atrophy; Calbindins; Cerebellum; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Humans; Immunohistochemistry; Infant, Newborn; Male; Methionine; Microscopy, Electron, Transmission; Muscle, Skeletal; Mutation; Neuroglia; Neurons; Phosphotransferases (Phosphomutases); S100 Calcium Binding Protein G; Threonine; Valine; Vimentin

2005
Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferase.
    Proceedings of the National Academy of Sciences of the United States of America, 1998, Oct-27, Volume: 95, Issue:22

    Topics: Cells, Cultured; Congenital Disorders of Glycosylation; Fibroblasts; Glucosyltransferases; Humans; Mannose; Mannose-6-Phosphate Isomerase; Methionine; Oligosaccharides; Phosphotransferases (Phosphomutases); Skin

1998